Desmoid tumor classification: Difference between revisions

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Revision as of 18:39, 21 January 2016

Desmoid tumor Microchapters

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Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Desmoid tumor from other Diseases

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

CT

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Faizan Sheraz, M.D. [2]

Overview

Classification

They can be divided into five subgroups: extraabdominal, , multiple, and as part of Gardner's syndrome. Extraabdominal desmoid tumors have a wide distribution; the shoulder girdle, trunk and lower extremities are most commonly involved. Abdominal desmoids, which may occur in the abdominal wall, or , have an increased incidence in individuals with Gardner syndrome.[1]

Classification Features

Extraabdominal

  • Wide distribution
  • Shoulder girdle
  • Trunk
  • Lower extremities

Intraabdominal

  • Mesentery
  • Retroperitoneum

Multiple Familial

  • Hereditary predisposition

Gardner Syndrome Associated

Turcot Syndrome Associated

  • Neural tumors



Reference

  1. Economou, Athanasios; Pitta, Xanthi; Andreadis, Efstathios; Papapavlou, Leonidas; Chrissidis, Thomas (2011). "Desmoid tumor of the abdominal wall: a case report". Journal of Medical Case Reports. 5 (1): 326. doi:10.1186/1752-1947-5-326. ISSN 1752-1947.

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